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Details
Link-It Detail - Human Phenotype - Abnormal hair laboratory examination
Debug Stats
  • ### Total Build Time: 42 ms 23.682 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 211 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 784 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.437 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.948 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 16.150 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal hair laboratory examination HP:0003328
Parents (2)
img Abnormality of the hair HP:0001595
img Abnormality of metabolism/homeostasis HP:0001939
Children (4)
img Pili torti HP:0003777
img Pili canaliculi HP:0002235
img Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes HP:0003329
img Trichorrhexis nodosa HP:0009886
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the hair HP:0001595
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the hair HP:0001595
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the hair HP:0001595
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanDSG4147409desmoglein 4
img HP RolledUp, OMIM ID: 607903
HumanPVRL481607poliovirus receptor-related 4
img HP RolledUp, OMIM ID: 613573
HumanHR55806hair growth associated
img HP RolledUp, OMIM ID: 146550
HumanHMU50823Hypotrichosis, Marie Unna type
img HP RolledUp, OMIM ID: 146550
HumanTTC379652tetratricopeptide repeat domain 37
img HP RolledUp, OMIM ID: 222470
HumanTP638626tumor protein p63
img HP RolledUp, OMIM ID: 129400
HumanBZX8255Bazex syndrome
img HP RolledUp, OMIM ID: 301845
HumanWRN7486Werner syndrome, RecQ helicase-like
img HP RolledUp, OMIM ID: 277700
HumanST146768suppression of tumorigenicity 14 (colon carcinoma)
img HP RolledUp, OMIM ID: 610765
HumanSKIV2L6499superkiller viralicidic activity 2-like (S. cerevisiae)
img HP RolledUp, OMIM ID: 614602
HumanPVRL15818poliovirus receptor-related 1 (herpesvirus entry mediator C)
img HP RolledUp, OMIM ID: 225060
HumanLMNA4000lamin A/C
img HP RolledUp, OMIM ID: 277700
HumanKRT853891keratin 85
img HP RolledUp, OMIM ID: 602032
HumanFOXE12304forkhead box E1 (thyroid transcription factor 2)
img HP RolledUp, OMIM ID: 241850
HumanERCC32071excision repair cross-complementing rodent repair deficiency, complementation group 3
img HP RolledUp, OMIM ID: 601675
HumanERCC22068excision repair cross-complementing rodent repair deficiency, complementation group 2
img HP RolledUp, OMIM ID: 601675
HumanCDH31001cadherin 3, type 1, P-cadherin (placental)
img HP RolledUp, OMIM ID: 601553
HumanBCS1L617BC1 (ubiquinol-cytochrome c reductase) synthesis-like
img HP RolledUp, OMIM ID: 262000
HumanASL435argininosuccinate lyase
img HP RolledUp, OMIM ID: 207900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003328Abnormal hair laboratory examination0self